The Implications of Primate Behavioral Flexibility for Sustainable Human–Primate Coexistence in Anthropogenic Habitats

Total Page:16

File Type:pdf, Size:1020Kb

The Implications of Primate Behavioral Flexibility for Sustainable Human–Primate Coexistence in Anthropogenic Habitats View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Oxford Brookes University: RADAR 1 THE IMPLICATIONS OF PRIMATE BEHAVIORAL FLEXIBILITY FOR SUSTAINABLE 2 HUMAN–PRIMATE COEXISTENCE IN ANTHROPOGENIC HABITATS 3 4 Matthew R. McLennan1,2, Noemi Spagnoletti3,4, Kimberley J. Hockings1,5 5 1 Anthropology Centre for Conservation, Environment and Development, Oxford Brookes University, 6 Oxford, OX3 0BP, UK 7 2 Bulindi Chimpanzee and Community Project, PO Box 245, Hoima, Uganda. 8 3 Department of Experimental Psychology, Institute of Psychology, University of São Paulo, São 9 Paulo, Brazil 10 4 Unit of Cognitive Primatology and Primate Center, Institute of Cognitive Sciences and Technologies, 11 CNR, Rome, Italy 12 5 Centre for Research in Anthropology (CRIA-FCSH/UNL), Lisbon, 1069-061, Portugal. 13 14 15 Running title: Primates in anthropogenic habitats 16 17 Corresponding author: 18 Dr Matthew McLennan 19 Faculty of Humanities and Social Sciences, 20 Oxford Brookes University, 21 Oxford OX3 0BP, 22 United Kingdom 23 Email: [email protected] 1 24 ABSTRACT 25 People are an inescapable aspect of most environments inhabited by nonhuman primates today. 26 Consequently, interest has grown in how primates adjust their behavior to live in anthropogenic 27 habitats. However, our understanding of primate behavioral flexibility and the degree to which it will 28 enable primates to survive alongside people in the long-term remains limited. This Special Issue 29 brings together a collection of papers that extend our knowledge of this subject. In this introduction, 30 we first review the literature to identify past and present trends in research, then introduce the 31 contributions to this Special Issue. Our literature review confirms that publications on primate 32 behavior in anthropogenic habitats, including interactions with people, increased markedly since the 33 2000s. Publications concern a diversity of primates but include only 17% of currently recognized 34 species, with certain primates over-represented in studies (e.g., chimpanzees and macaques). 35 Primates exhibit behavioral flexibility in anthropogenic habitats in various ways, most commonly 36 documented as dietary adjustments (i.e., incorporation of human foods including agricultural crops 37 and other exotic plants, and provisioned items) and differences in activity, ranging, grouping 38 patterns, and social organization, associated with changing anthropogenic factors. Publications are 39 more likely to include information on negative rather than positive or neutral interactions between 40 humans and primates. The contributions to this Special Issue include both empirical research and 41 reviews that examine various aspects of the human–primate interface. Collectively, they show that 42 primate behavior in shared landscapes does not always conflict with human interests, and 43 demonstrate the value of examining behavior from a cost–benefit perspective without making prior 44 assumptions concerning the nature of interactions. Careful interdisciplinary research has the 45 potential to greatly improve our understanding of the complexities of human–primate interactions, 46 and is crucial for identifying appropriate mechanisms to enable sustainable human–primate 47 coexistence in the 21st Century and beyond. 48 2 49 Keywords: Anthropocene, behavioral adaptability, behavioral plasticity, ethnoprimatology, human- 50 dominated landscapes, human–wildlife interactions 3 51 INTRODUCTION 52 Flexible behavior – sometimes referred to as ‘adaptability’ or ‘plasticity’, although these terms are 53 not strictly synonyms (Strier 2017) – evolves in response to heterogeneous environments (Jones 54 2005). An animal’s ability to adjust its behavior under changing conditions can determine its survival 55 in a fast-changing world dominated by humans (Wong and Candolin 2015). Until quite recently, how 56 nonhuman primates (hereafter referred to as ‘primates’) respond behaviorally to human-induced 57 environmental changes and increased contact with people was not a primary focus of research (but 58 see Horrocks and Hunte 1986; Kavanagh 1980; Maples et al. 1976 for early examples of such work). 59 However, rapid human population growth and associated land-use changes such as agriculture and 60 urbanization are transforming primate habitats (Estrada et al. 2012; McKinney 2015). Consequently, 61 much field primatology today is conducted in ‘anthropogenic habitats’, a broad term which is 62 equivalent to ‘human-dominated’ or ‘human-impacted’ habitats, among similar terms (see McKinney 63 2015 for detailed analysis of anthropogenic influences on primate habitats). With the acceptance 64 that modified environments offer habitat for many primates, theoretical and applied interest in how 65 primates behave in anthropogenic habitats has increased (Hockings et al. 2015; Humle and Hill 2016; 66 Nowak and Lee 2013; Strier 2017). 67 Consistent with the wider literature on human–wildlife interactions (Angelici 2016; Seoraj- 68 Pillai and Pillay 2017; Woodroffe et al. 2005), research on primates in anthropogenic habitats has 69 tended to concentrate on negative aspects of human–primate interactions, such as primates 70 ‘raiding’ agricultural crops and other ‘conflicts’ that challenge the sustainability of primate 71 coexistence with people (Hill 2005). This reminds us that not all behavioral adjustments to 72 anthropogenic habitats are beneficial (see Sih et al. 2011; Tuomainen and Candolin 2011; Wong and 73 Candolin 2015), with some behaviors compromising the survival of primate populations, for example 74 by inciting persecution by people. Understanding primates’ behavioral flexibility in response to 75 human influence on their habitat, and how local people perceive and respond to changing primate 4 76 behavior, can inform conservation management to aid the long-term survival of primates in a fast- 77 changing world (Hockings et al. 2015; Nowak and Lee 2013). 78 To explore these issues in more depth, we organized a Symposium entitled “Behavioral 79 flexibility by primates in anthropogenic habitats” at the VIth European Federation for Primatology 80 Congress held in Rome in August 2015, inviting presentations from researchers studying human– 81 primate interactions. In response to the interest shown during the symposium, Joanna M. Setchell, 82 Editor-in-Chief of the International Journal of Primatology, invited us to guest edit a Special Issue on 83 this topic. This Special Issue presents papers which illustrate different and novel ways that primates 84 exhibit behavioral flexibility in response to human-induced habitat changes, and how this affects the 85 long-term sustainability of their interactions with humans. We refer to these themes more generally 86 in this introduction as “primates in anthropogenic habitats”. To provide context to the contributions, 87 we first reviewed the literature to identify past and present trends in research focus in primates in 88 anthropogenic habitats. We discuss which primates are most studied and where, what kinds of 89 behavioral adjustments are reported, and the nature of interactions reported between primates and 90 people, with representative examples from the literature search. Next, we introduce the 91 contributions to this Special Issue. We conclude with reflections on the current state of research in 92 this evolving field, and suggest future lines of inquiry for its development. 93 94 RESEARCH TRENDS 95 We searched the literature for publications reporting primate behavior in anthropogenic habitats 96 using the Web of ScienceTM database. We searched using ‘All Databases’, which included the Web of 97 Science core collection, MEDLINE, and BIOSIS and SciELO citation indexes, covering articles published 98 from 1970 to December 7th 2016. We searched for full-length research articles, short 99 communications, commentaries and reviews, but excluded studies published as abstracts only. We 100 used the key words ‘primate’, ‘monkey’, ‘ape’ and ‘lemur’ in all searches, as well as common names 101 (e.g., macaque, baboon, capuchin, chimpanzee) in some searches. We combined key words with 5 102 relevant search terms, repeating searches using alternative or synonymous terms. Search terms that 103 returned greatest numbers of relevant articles were human–wildlife conflict, human–wildlife 104 interactions, crops, crop raiding, agriculture, plantation, anthropogenic, human-dominated, tourism, 105 provisioning, and urban. 106 Our criterion for inclusion was that articles include information on any of the following: (i) 107 primate behaviors that may be regarded as adjustments to, or consequences of, living in 108 anthropogenic habitats, and thus broadly indicative of flexibility in such environments. While 109 behavioral ‘adjustments’ included reports of differences between primates in anthropogenic 110 habitats compared to those in less human-impacted ones, we refer to these behavioral differences 111 as ‘adjustments’ for consistency with the wider literature (e.g., Sol et al. 2013; Wong and Candolin 112 2015). Reported adjustments include behaviors associated with diet (i.e., feeding on exotic items), 113 activity, ranging, social organization and reproduction; (ii) behavioral responses of primates to novel 114 aspects of, or risks associated with, anthropogenic habitats; (iii) direct interactions between 115 primates and humans in anthropogenic habitats (tourists, local people or researchers); (iv) human 116 perceptions of, attitudes
Recommended publications
  • The Behavioral Ecology of the Tibetan Macaque
    Fascinating Life Sciences Jin-Hua Li · Lixing Sun Peter M. Kappeler Editors The Behavioral Ecology of the Tibetan Macaque Fascinating Life Sciences This interdisciplinary series brings together the most essential and captivating topics in the life sciences. They range from the plant sciences to zoology, from the microbiome to macrobiome, and from basic biology to biotechnology. The series not only highlights fascinating research; it also discusses major challenges associ- ated with the life sciences and related disciplines and outlines future research directions. Individual volumes provide in-depth information, are richly illustrated with photographs, illustrations, and maps, and feature suggestions for further reading or glossaries where appropriate. Interested researchers in all areas of the life sciences, as well as biology enthu- siasts, will find the series’ interdisciplinary focus and highly readable volumes especially appealing. More information about this series at http://www.springer.com/series/15408 Jin-Hua Li • Lixing Sun • Peter M. Kappeler Editors The Behavioral Ecology of the Tibetan Macaque Editors Jin-Hua Li Lixing Sun School of Resources Department of Biological Sciences, Primate and Environmental Engineering Behavior and Ecology Program Anhui University Central Washington University Hefei, Anhui, China Ellensburg, WA, USA International Collaborative Research Center for Huangshan Biodiversity and Tibetan Macaque Behavioral Ecology Anhui, China School of Life Sciences Hefei Normal University Hefei, Anhui, China Peter M. Kappeler Behavioral Ecology and Sociobiology Unit, German Primate Center Leibniz Institute for Primate Research Göttingen, Germany Department of Anthropology/Sociobiology University of Göttingen Göttingen, Germany ISSN 2509-6745 ISSN 2509-6753 (electronic) Fascinating Life Sciences ISBN 978-3-030-27919-6 ISBN 978-3-030-27920-2 (eBook) https://doi.org/10.1007/978-3-030-27920-2 This book is an open access publication.
    [Show full text]
  • Dietary Adaptations of Assamese Macaques (Macaca Assamensis) in Limestone Forests in Southwest China
    American Journal of Primatology 77:171–185 (2015) RESEARCH ARTICLE Dietary Adaptations of Assamese Macaques (Macaca assamensis)in Limestone Forests in Southwest China ZHONGHAO HUANG1,2, CHENGMING HUANG3, CHUANGBIN TANG4, LIBIN HUANG2, 5 1,6 2 HUAXING TANG , GUANGZHI MA *, AND QIHAI ZHOU ** 1School of Life Sciences, South China Normal University, Guangzhou, China 2Guangxi Key Laboratory of Rare and Endangered Animal Ecology, Guangxi Normal University, Guilin, China 3National Zoological Museum, Institute of Zoology, Chinese Academy of Sciences, Beijing, China 4College of Forest Resources and Environment, Nanjing Forestry University, Nanjing, China 5The Administration of Nonggang Nature Reserve, Chongzuo, China 6Guangdong Institute of Science and Technology, Zhuhai, China Limestone hills are an unusual habitat for primates, prompting them to evolve specific behavioral adaptations to the component karst habitat. From September 2012 to August 2013, we collected data on the diet of one group of Assamese macaques living in limestone forests at Nonggang National Nature Reserve, Guangxi Province, China, using instantaneous scan sampling. Assamese macaques were primarily folivorous, young leaves accounting for 75.5% and mature leaves an additional 1.8% of their diet. In contrast, fruit accounted for only 20.1%. The young leaves of Bonia saxatilis, a shrubby, karst‐ endemic bamboo that is superabundant in limestone hills, comprised the bulk of the average monthly diet. Moreover, macaques consumed significantly more bamboo leaves during the season when the availability of fruit declined, suggesting that bamboo leaves are an important fallback food for Assamese macaques in limestone forests. In addition, diet composition varied seasonally. The monkeys consumed significantly more fruit and fewer young leaves in the fruit‐rich season than in the fruit‐lean season.
    [Show full text]
  • Sex-Specific Variation of Social Play in Wild Immature Tibetan Macaques
    animals Article Sex-Specific Variation of Social Play in Wild Immature Tibetan Macaques, Macaca thibetana Tong Wang 1,2, Xi Wang 2,3, Paul A. Garber 4,5, Bing-Hua Sun 2,3, Lixing Sun 6, Dong-Po Xia 1,2,* and Jin-Hua Li 2,3,* 1 School of Life Sciences, Anhui University, Hefei 230601, China; [email protected] 2 International Collaborative Research Center for Huangshan Biodiversity and Tibetan Macaque Behavioral Ecology, Hefei 230601, China; [email protected] (X.W.); [email protected] (B.-H.S.) 3 School of Resource and Environmental Engineering, Anhui University, Hefei 230601, China 4 Department of Anthropology and Program in Ecology, Evolution, and Conservation Biology, University of Illinois, Urbana, IL 61801, USA; [email protected] 5 International Centre of Biodiversity and Primate Conservation, Dali University, Dali 671000, China 6 Department of Biology, Central Washington University, Ellensburg, WA 98926, USA; [email protected] * Correspondence: [email protected] (D.-P.X.); [email protected] (J.-H.L.); Tel.: +86-551-63861723 (D.-P.X. & J.-H.L.) Simple Summary: Social play among immature individuals has been well-documented across a wide range of mammalian species. It represents a substantial part of the daily behavioral repertoire during immature periods, and it is essential for acquiring an appropriate set of motor, cognitive, and social skills. In this study, we found that infant Tibetan macaques (Macaca thibetana) exhibited similar patterns of social play between males and females, juvenile males engaged more aggressive play than juvenile females, and juvenile females engaged more affiliative play than juvenile males.
    [Show full text]
  • Macaca Thibetana)
    ZOOLOGICAL RESEARCH Interchange between grooming and infant handling in female Tibetan macaques (Macaca thibetana) Qi Jiang1, Dong-Po Xia2, Xi Wang1, Dao Zhang1, Bing-Hua Sun1, Jin-Hua Li1,3,* 1 School of Resource and Environmental Engineering, Anhui University, Hefei Anhui 230601, China 2 School of Life Science, Anhui University, Hefei Anhui 230601, China 3 School of Life Science, Hefei Normal University, Hefei Anhui 241000, China ABSTRACT Keywords: Tibetan macaques (Macaca thibetana); Interchange; Infant handling; Grooming; Biological In some non-human primates, infants function as market theory a social tool that can bridge relationships among INTRODUCTION group members. Infants are a desired commodity for group members, and mothers control access to While female attraction to infants represents a common feature them. The biological market theory suggests that in non-human primate species, maternal responses to infant handling show a certain degree of variability (Maestripieri, grooming is widespread and represents a commodity 1994; Nicolson, 1987). In some species, such as Asian that can be exchanged for infant handling. As colobines, females allow their newborn infants to be held a limited resource, however, the extent to which frequently and carried for long durations by other group infants are interchanged between mothers (females members (infant caretaking) (Nicolson, 1987; Stanford, 1992). with an infant) and non-mothers (potential handlers, In other species, such as baboons and macaques, mothers are much more restrictive in allowing access their young females without an infant) remains unclear. In this offspring (Altmann, 2002; Nicolson, 1987), despite persistent study, we collected behavioral data to investigate the attempts by group members to interact with their infant (Frank relationship between grooming and infant handling in & Silk, 2009; Gumert, 2007a; Henzi & Barrett, 2002).
    [Show full text]
  • World's Most Endangered Primates
    Primates in Peril The World’s 25 Most Endangered Primates 2016–2018 Edited by Christoph Schwitzer, Russell A. Mittermeier, Anthony B. Rylands, Federica Chiozza, Elizabeth A. Williamson, Elizabeth J. Macfie, Janette Wallis and Alison Cotton Illustrations by Stephen D. Nash IUCN SSC Primate Specialist Group (PSG) International Primatological Society (IPS) Conservation International (CI) Bristol Zoological Society (BZS) Published by: IUCN SSC Primate Specialist Group (PSG), International Primatological Society (IPS), Conservation International (CI), Bristol Zoological Society (BZS) Copyright: ©2017 Conservation International All rights reserved. No part of this report may be reproduced in any form or by any means without permission in writing from the publisher. Inquiries to the publisher should be directed to the following address: Russell A. Mittermeier, Chair, IUCN SSC Primate Specialist Group, Conservation International, 2011 Crystal Drive, Suite 500, Arlington, VA 22202, USA. Citation (report): Schwitzer, C., Mittermeier, R.A., Rylands, A.B., Chiozza, F., Williamson, E.A., Macfie, E.J., Wallis, J. and Cotton, A. (eds.). 2017. Primates in Peril: The World’s 25 Most Endangered Primates 2016–2018. IUCN SSC Primate Specialist Group (PSG), International Primatological Society (IPS), Conservation International (CI), and Bristol Zoological Society, Arlington, VA. 99 pp. Citation (species): Salmona, J., Patel, E.R., Chikhi, L. and Banks, M.A. 2017. Propithecus perrieri (Lavauden, 1931). In: C. Schwitzer, R.A. Mittermeier, A.B. Rylands, F. Chiozza, E.A. Williamson, E.J. Macfie, J. Wallis and A. Cotton (eds.), Primates in Peril: The World’s 25 Most Endangered Primates 2016–2018, pp. 40-43. IUCN SSC Primate Specialist Group (PSG), International Primatological Society (IPS), Conservation International (CI), and Bristol Zoological Society, Arlington, VA.
    [Show full text]
  • Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes As in Mandrill
    Send Orders for Reprints to [email protected] Current Genomics, 2018, 19, 207-215 207 RESEARCH ARTICLE Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes as in Mandrill Wiwat Sangpakdee1,2, Alongkoad Tanomtong2, Arunrat Chaveerach2, Krit Pinthong1,2,3, Vladimir Trifonov1,4, Kristina Loth5, Christiana Hensel6, Thomas Liehr1,*, Anja Weise1 and Xiaobo Fan1 1Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, D-07747 Jena, Germany; 2Department of Biology Faculty of Science, Khon Kaen University, 123 Moo 16 Mittapap Rd., Muang Dis- trict, Khon Kaen 40002, Thailand; 3Faculty of Science and Technology, Surindra Rajabhat University, 186 Moo 1, Maung District, Surin 32000, Thailand; 4Institute of Molecular and Cellular Biology, Lavrentev Str. 8/2, Novosibirsk 630090, Russian Federation; 5Serengeti-Park Hodenhagen, Am Safaripark 1, D-29693 Hodenhagen, Germany; 6Thüringer Zoopark Erfurt, Am Zoopark 1, D-99087 Erfurt, Germany Abstract: Background: The question how evolution and speciation work is one of the major interests of biology. Especially, genetic including karyotypic evolution within primates is of special interest due to the close phylogenetic position of Macaca and Homo sapiens and the role as in vivo models in medical research, neuroscience, behavior, pharmacology, reproduction and Acquired Immune Defi- ciency Syndrome (AIDS). Material & Methods: Karyotypes of five macaque species from South East Asia and of one macaque A R T I C L E H I S T O R Y species as well as mandrill from Africa were analyzed by high resolution molecular cytogenetics to obtain new insights into karyotypic evolution of old world monkeys.
    [Show full text]
  • Primate Conservation 2006 (20): 1–28
    Contents General Primates in Peril: The World’s 25 Most Endangered Primates, 2004–2006 ..................................................................................1 Russell A. Mittermeier, Cláudio Valladares-Pádua, Anthony B. Rylands, Ardith A. Eudey, Thomas M. Butynski, Jörg U. Ganzhorn, Rebecca Kormos, John M. Aguiar and Sally Walker Neotropical Region On a New Species of Titi Monkey, Genus Callicebus Thomas (Primates, Pitheciidae), from Western Bolivia with Preliminary Notes on Distribution and Abundance ...............................................................................................................29 Robert. B. Wallace, Humberto Gómez, Annika Felton and Adam M. Felton Identifi cation, Behavioral Observations, and Notes on the Distribution of the Titi Monkeys Callicebus modestus Lönnberg, 1939 and Callicebus olallae Lönnberg, 1939 ..............................................................................41 Adam Felton, Annika M. Felton, Robert B. Wallace and Humberto Gómez A Survey of Primate Populations in Northeastern Venezuelan Guayana .....................................................................................47 Bernardo Urbani A History of Long-term Research and Conservation of Northern Muriquis (Brachyteles hypoxanthus) at the Estação Biológica de Caratinga/RPPN-FMA .......................................................................................................................53 Karen B. Strier and Jean Philippe Boubli Africa English Common Names for Subspecies and Species of African Primates
    [Show full text]
  • Tibetan Macaques with Higher Social Centrality and More Relatives Emit More Frequent Visual Communication in Collective Decision-Making
    animals Article Tibetan Macaques with Higher Social Centrality and More Relatives Emit More Frequent Visual Communication in Collective Decision-Making Zifei Tang 1,2, Xi Wang 1,2,*, Mingyang Wu 2,3, Shiwang Chen 2,3 and Jinhua Li 1,2,4,* 1 School of Resources and Environmental Engineering, Anhui University, Hefei 230601, China; [email protected] 2 International Collaborative Research Center for Huangshan Biodiversity and Tibetan Macaque Behavior Ecology, Hefei 230601, China; [email protected] (M.W.); [email protected] (S.C.) 3 School of Life Sciences, Anhui University, Hefei 230601, China 4 School of Life Sciences, Hefei Normal University, Hefei 230601, China * Correspondence: [email protected] (X.W.); [email protected] (J.L.) Simple Summary: It is well known that visual communication plays an important role in collective decision-making. However, there is not much research on the influencing factors of visual signals, especially kinship and social relations. In this study, we not only confirmed the function of visual communication in collective decision-making, but also found the effect of kinship and social relations on visual communication. Tibetan macaques with higher social centrality and more relatives emit more frequent visual communication, providing a reference for further research on decision-making. Understanding the link between communication and decision-making can elucidate the powers of group maintenance in animal societies. Citation: Tang, Z.; Wang, X.; Wu, M.; Chen, S.; Li, J. Tibetan Macaques with Abstract: Animals on the move often communicate with each other through some specific postures. Higher Social Centrality and More Previous studies have shown that social interaction plays a role in communication process.
    [Show full text]
  • OPTIMAL FORAGING on the ROOF of the WORLD: a FIELD STUDY of HIMALAYAN LANGURS a Dissertation Submitted to Kent State University
    OPTIMAL FORAGING ON THE ROOF OF THE WORLD: A FIELD STUDY OF HIMALAYAN LANGURS A dissertation submitted to Kent State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy by Kenneth A. Sayers May 2008 Dissertation written by Kenneth A. Sayers B.A., Anderson University, 1996 M.A., Kent State University, 1999 Ph.D., Kent State University, 2008 Approved by ____________________________________, Dr. Marilyn A. Norconk Chair, Doctoral Dissertation Committee ____________________________________, Dr. C. Owen Lovejoy Member, Doctoral Dissertation Committee ____________________________________, Dr. Richard S. Meindl Member, Doctoral Dissertation Committee ____________________________________, Dr. Charles R. Menzel Member, Doctoral Dissertation Committee Accepted by ____________________________________, Dr. Robert V. Dorman Director, School of Biomedical Sciences ____________________________________, Dr. John R. D. Stalvey Dean, College of Arts and Sciences ii TABLE OF CONTENTS LIST OF FIGURES ............................................................................................... vi LIST OF TABLES ............................................................................................... viii ACKNOWLEDGEMENTS .....................................................................................x Chapter I. PRIMATES AT THE EXTREMES ..................................................1 Introduction: Primates in marginal habitats ......................................1 Prosimii .............................................................................................2
    [Show full text]
  • List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
    What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34.
    [Show full text]
  • View / Open Gartland Oregon 0171A 12939.Pdf
    MALE JAPANESE MACAQUE (MACACA FUSCATA) SOCIALITY: BEHAVIORAL STRATEGIES AND WELFARE SCIENCE APPLICATIONS by KYLEN NADINE GARTLAND A DISSERTATION Presented to the Department of Anthropology and the Graduate School of the University of Oregon in partial fulfillment of the requirements for the degree of Doctor of Philosophy March 2021 DISSERTATION APPROVAL PAGE Student: Kylen Nadine Gartland Title: Male Japanese Macaque (Macaca fuscata) Sociality: Behavioral Strategies and Welfare Science Applications This dissertation has been accepted and approved in partial fulfillment of the requirements for the Doctor of Philosophy degree in the Department of Anthropology by: Frances White Chairperson Lawrence Ulibarri Core Member Steve Frost Core Member Renee Irvin Institutional Representative and Kate Mondlock Interim Vice Provost and Dean of the Graduate School Original approval signatures are on file with the University of Oregon Graduate School. Degree awarded March 2021 ii © 2021 Kylen Nadine Gartland iii DISSERTATION ABSTRACT Kylen Nadine Gartland Doctor of Philosophy Department of Anthropology February 2021 Title: Male Japanese macaque (Macaca fuscata) sociality: Behavioral strategies and welfare science application Evolutionarily, individuals should pursue social strategies which confer advantages such as coalitionary support, mating opportunities, or access to limited resources. How an individual forms and maintains social bonds may be influenced by a large number of factors including sex, age, dominance rank, group structure, group demographics, relatedness, or seasonality. Individuals may employ differential social strategies both in terms of the type and quantity of interactions they engage in as well as their chosen social partners. The objective of this dissertation is to examine sociality in adult male Japanese macaques (Macaca fuscata) and the varying strategies that individuals may employ depending on their relative position within a social group.
    [Show full text]
  • First Open Access Ensemble Climate Envelope Predictions of Assamese Macaque Macaca Assamensis in Asia: a New Role Model and Assessment of Endangered Species
    Vol. 36: 149–160, 2018 ENDANGERED SPECIES RESEARCH Published July 10 https://doi.org/10.3354/esr00888 Endang Species Res OPEN ACCESS First open access ensemble climate envelope predictions of Assamese macaque Macaca assamensis in Asia: a new role model and assessment of endangered species Ganga Ram Regmi1, Falk Huettmann2,*, Madan Krishna Suwal1,3, Vincent Nijman4, K. A. I. Nekaris4, Kamal Kandel1, Narayan Sharma5,6, Camille Coudrat4 1Global Primate Network-Nepal, GPO Box 26288, Kathmandu, Nepal 2EWHALE lab, Institute of Arctic Biology, Biology and Wildlife Department, University of Alaska Fairbanks (UAF), Fairbanks, Alaska 99775, USA 3Department of Geography, University of Bergen, Fosswinckelsgt 6, PB 7802, 5020 Bergen, Norway 4Oxford Brookes University, Oxford, OX3 0BP, UK 5Department of Environmental Biology and Wildlife Sciences, Cotton College State University, Pan Bazar, Guwahati 781001, Assam, India 6School of Natural Sciences and Engineering, National Institute of Advanced Studies, Indian Institute of Science Campus, Bengaluru 560012, Karnataka, India ABSTRACT: Species distribution models are a key component for understanding a species’ poten- tial occurrence, specifically in vastly undersampled landscapes. The current species distribution data for the Assamese macaque Macaca assamensis are outdated, but suggest a patchy distribu- tion in moist broadleaved forests in South and Southeast Asia. Therefore, in this study, we used a species distribution model to explore the potential climatic niche of this species and assess its distribution and potential barriers in 12 South and Southeast Asian countries. We combined primary and secondary species occurrence records from different countries. We applied Classifi- cation and Regression Tree (CART), TreeNet (boosting), RandomForest (bagging) and Maximum Entropy (MaxEnt) machine-learning algorithms with elevation as well as 19 bioclimatic variables for the first ensemble predictions ever completed for this species.
    [Show full text]